Variant (rsID / SNP)

rs397515831

rs397515831 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,729,989. Clinical significance in the table: Likely pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FBN1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 15:48729989
Cytoband: 15q21.1
HGVS: NM_000138.5(FBN1):c.6289G>T (p.Glu2097Ter)
Allele change: Nonsense_E2097X

Associated conditions / phenotypes

Marfan syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.